• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
miR-20b downregulates polymerases κ and θ in XP-V tumor cells.微小RNA-20b下调着色性干皮病变异型肿瘤细胞中的聚合酶κ和θ。
Oncol Lett. 2016 Jun;11(6):3790-3794. doi: 10.3892/ol.2016.4447. Epub 2016 Apr 18.
2
A novel mutation causes XP-V disease and XP-V tumor proneness may involve imbalance of numerous DNA polymerases.一种新的突变导致着色性干皮病V型,且着色性干皮病V型的肿瘤易感性可能涉及多种DNA聚合酶的失衡。
Oncol Lett. 2013 Dec;6(6):1583-1590. doi: 10.3892/ol.2013.1604. Epub 2013 Oct 7.
3
Translesion replication in cisplatin-treated xeroderma pigmentosum variant cells is also caffeine-sensitive: features of the error-prone DNA polymerase(s) involved in UV-mutagenesis.顺铂处理的着色性干皮病变异细胞中的跨损伤复制对咖啡因也敏感:紫外线诱变中涉及的易出错DNA聚合酶的特征。
DNA Repair (Amst). 2003 Aug 12;2(8):909-24. doi: 10.1016/s1568-7864(03)00092-2.
4
MicroRNA-20b inhibits trophoblast cell migration and invasion by targeting MMP-2.微小RNA-20b通过靶向基质金属蛋白酶-2抑制滋养层细胞迁移和侵袭。
Int J Clin Exp Pathol. 2017 Nov 1;10(11):10901-10909. eCollection 2017.
5
Differential distribution of miR-20a and miR-20b may underly metastatic heterogeneity of breast cancers.miR-20a和miR-20b的差异分布可能是乳腺癌转移异质性的基础。
Asian Pac J Cancer Prev. 2012;13(5):1901-6. doi: 10.7314/apjcp.2012.13.5.1901.
6
miR-20b promotes cellular proliferation and migration by directly regulating phosphatase and tensin homolog in prostate cancer.微小RNA-20b通过直接调控前列腺癌中的磷酸酶及张力蛋白同源物来促进细胞增殖和迁移。
Oncol Lett. 2017 Dec;14(6):6895-6900. doi: 10.3892/ol.2017.7041. Epub 2017 Sep 25.
7
MicroRNA-20b promotes proliferation of H22 hepatocellular carcinoma cells by targeting PTEN.微小RNA-20b通过靶向PTEN促进H22肝癌细胞的增殖。
Oncol Lett. 2019 Mar;17(3):2931-2936. doi: 10.3892/ol.2019.9925. Epub 2019 Jan 14.
8
Xeroderma pigmentosum variant and error-prone DNA polymerases.着色性干皮病变异型与易出错的DNA聚合酶。
Biochimie. 2003 Nov;85(11):1123-32. doi: 10.1016/j.biochi.2003.10.009.
9
Regulation of BTG3 by microRNA-20b-5p in non-small cell lung cancer.非小细胞肺癌中微小RNA-20b-5p对BTG3的调控
Oncol Lett. 2019 Jul;18(1):137-144. doi: 10.3892/ol.2019.10333. Epub 2019 May 7.
10
Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity.来自人宫颈癌细胞系的着色性干皮病变异型(XP-V)校正蛋白具有胸腺嘧啶二聚体旁路DNA聚合酶活性。
EMBO J. 1999 Jun 15;18(12):3491-501. doi: 10.1093/emboj/18.12.3491.

引用本文的文献

1
Maintenance of Genome Integrity: How Mammalian Cells Orchestrate Genome Duplication by Coordinating Replicative and Specialized DNA Polymerases.基因组完整性的维持:哺乳动物细胞如何通过协调复制性和特异性DNA聚合酶来编排基因组复制
Genes (Basel). 2017 Jan 6;8(1):19. doi: 10.3390/genes8010019.

本文引用的文献

1
A novel mutation causes XP-V disease and XP-V tumor proneness may involve imbalance of numerous DNA polymerases.一种新的突变导致着色性干皮病V型,且着色性干皮病V型的肿瘤易感性可能涉及多种DNA聚合酶的失衡。
Oncol Lett. 2013 Dec;6(6):1583-1590. doi: 10.3892/ol.2013.1604. Epub 2013 Oct 7.
2
DNA polymerase zeta cooperates with polymerases kappa and iota in translesion DNA synthesis across pyrimidine photodimers in cells from XPV patients.在着色性干皮病患者的细胞中,DNA聚合酶ζ与聚合酶κ和ι协同作用,进行跨嘧啶光二聚体的跨损伤DNA合成。
Proc Natl Acad Sci U S A. 2009 Jul 14;106(28):11552-7. doi: 10.1073/pnas.0812548106. Epub 2009 Jun 29.
3
The impact of microRNAs on protein output.微小RNA对蛋白质产出的影响。
Nature. 2008 Sep 4;455(7209):64-71. doi: 10.1038/nature07242. Epub 2008 Jul 30.
4
Xeroderma pigmentosum-variant patients from America, Europe, and Asia.来自美国、欧洲和亚洲的着色性干皮病变异型患者。
J Invest Dermatol. 2008 Aug;128(8):2055-68. doi: 10.1038/jid.2008.48. Epub 2008 Mar 27.
5
DNA polymerases eta and theta function in the same genetic pathway to generate mutations at A/T during somatic hypermutation of Ig genes.DNA聚合酶η和θ在同一条遗传途径中发挥作用,在Ig基因的体细胞超突变过程中于A/T位点产生突变。
J Biol Chem. 2007 Jun 15;282(24):17387-94. doi: 10.1074/jbc.M611849200. Epub 2007 Apr 20.
6
Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type.对被诊断为着色性干皮病变异型的日本患者的DNA聚合酶η基因进行分子分析。
J Invest Dermatol. 2007 Jul;127(7):1745-51. doi: 10.1038/sj.jid.5700759. Epub 2007 Mar 8.
7
Vertebrate POLQ and POLbeta cooperate in base excision repair of oxidative DNA damage.脊椎动物的POLQ和POLβ在氧化性DNA损伤的碱基切除修复中相互协作。
Mol Cell. 2006 Oct 6;24(1):115-25. doi: 10.1016/j.molcel.2006.07.032.
8
Oncomirs - microRNAs with a role in cancer.癌基因miRNA——在癌症中发挥作用的微小RNA。
Nat Rev Cancer. 2006 Apr;6(4):259-69. doi: 10.1038/nrc1840.
9
MicroRNAs: genomics, biogenesis, mechanism, and function.微小RNA:基因组学、生物发生、作用机制及功能
Cell. 2004 Jan 23;116(2):281-97. doi: 10.1016/s0092-8674(04)00045-5.
10
Molecular genetics of Xeroderma pigmentosum variant.着色性干皮病变异型的分子遗传学
Exp Dermatol. 2003 Oct;12(5):529-36. doi: 10.1034/j.1600-0625.2003.00124.x.

微小RNA-20b下调着色性干皮病变异型肿瘤细胞中的聚合酶κ和θ。

miR-20b downregulates polymerases κ and θ in XP-V tumor cells.

作者信息

Guo Jia, Jiang Zheng, Li Xiangru, Wang X I, Xiao Yan

机构信息

Department of Endodontics, Oral Medical Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.

Department of Endodontics, Xiamen Stomatological Hospital, Xiamen, Fujian 361004, P.R. China.

出版信息

Oncol Lett. 2016 Jun;11(6):3790-3794. doi: 10.3892/ol.2016.4447. Epub 2016 Apr 18.

DOI:10.3892/ol.2016.4447
PMID:27313696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4888293/
Abstract

XP-V is a subtype of Xeroderma pigmentosum diseases with typical pigmentation and cancers in sun-exposed regions. The present study investigated the role of microRNA-20b (miR-20b) in the imbalance of polymerase expression levels in XP-V tumor cells. Following software prediction results, certain miRNAs were chosen as candidate regulators for the observed imbalance in polymerases in XP-V tumor cells. Reverse transcription-quantitative polymerase chain reaction and western blot were used to test candidate miRNAs for their ability to reduce the expression of these polymerases. A luciferase reporter assay was used to further verify the western blot results. Polymerases κ and θ were expressed at lower levels in XP-V tumor cells compared to normal control cells. A positive correlation was demonstrated between miR-20b and polymerases κ and θ. It was also demonstrated that a proportion of miRNAs had no effect on polymerases κ and θ, despite the software predicting that these miRNAs would target these two polymerases. Therefore, miR-20b may be responsible for the low expression levels of polymerase κ and θ in XP-V tumor cells, which accelerated mismatch in DNA replication repairing.

摘要

着色性干皮病变异型(XP-V)是着色性干皮病的一种亚型,在阳光暴露部位有典型的色素沉着和癌症。本研究调查了微小RNA-20b(miR-20b)在XP-V肿瘤细胞中聚合酶表达水平失衡中的作用。根据软件预测结果,选择了某些微小RNA作为XP-V肿瘤细胞中观察到的聚合酶失衡的候选调节因子。采用逆转录定量聚合酶链反应和蛋白质印迹法检测候选微小RNA降低这些聚合酶表达的能力。使用荧光素酶报告基因检测进一步验证蛋白质印迹结果。与正常对照细胞相比,XP-V肿瘤细胞中聚合酶κ和θ的表达水平较低。miR-20b与聚合酶κ和θ之间呈正相关。还证明,尽管软件预测这些微小RNA会靶向这两种聚合酶,但一部分微小RNA对聚合酶κ和θ没有影响。因此,miR-20b可能是XP-V肿瘤细胞中聚合酶κ和θ低表达水平的原因,这加速了DNA复制修复中的错配。